388 related articles for article (PubMed ID: 17063531)
1. Rapid prenatal diagnosis of common trisomies: discordant results between QF-PCR analysis and karyotype analysis on long-term culture for a case of trisomy 18 detected in CVS.
Allen SK; Luharia A; Gould CP; MacDonald F; Larkins S; Davison EV
Prenat Diagn; 2006 Dec; 26(12):1160-7. PubMed ID: 17063531
[TBL] [Abstract][Full Text] [Related]
2. Detection of mosaicism for primary trisomies in prenatal samples by QF-PCR and karyotype analysis.
Donaghue C; Mann K; Docherty Z; Ogilvie CM
Prenat Diagn; 2005 Jan; 25(1):65-72. PubMed ID: 15662691
[TBL] [Abstract][Full Text] [Related]
3. Complete discrepancy between QF-PCR analysis of uncultured villi and karyotyping of cultured cells in the prenatal diagnosis of trisomy 21 in three CVS.
Waters JJ; Mann K; Grimsley L; Ogilvie CM; Donaghue C; Staples L; Hills A; Adams T; Wilson C
Prenat Diagn; 2007 Apr; 27(4):332-9. PubMed ID: 17286305
[TBL] [Abstract][Full Text] [Related]
4. Complete discrepancy between abnormal fetal karyotypes predicted by QF-PCR rapid testing and karyotyped cultured cells in a first-trimester CVS.
Waters JJ; Walsh S; Levett LJ; Liddle S; Akinfenwa Y
Prenat Diagn; 2006 Oct; 26(10):892-7. PubMed ID: 16906600
[TBL] [Abstract][Full Text] [Related]
5. [Application of multiplex quantitative fluorescent PCR with non-polymorphic loci in prenatal diagnosis].
Zhu XY; Hu YL; Wang YP; Zhu HY; Li J; Zhu RF; Zhang Y; Wu X; Yang Y
Zhonghua Fu Chan Ke Za Zhi; 2008 Nov; 43(11):818-23. PubMed ID: 19087563
[TBL] [Abstract][Full Text] [Related]
6. Assessing discrepant findings between QF-PCR on uncultured prenatal samples and karyotyping on long-term culture.
Lau ET; Tang L; Wong C; Yung Hang L; Ghosh A; Leung WC; Sin WK; Lau TK; Kung YY; Tang MH
Prenat Diagn; 2009 Feb; 29(2):151-5. PubMed ID: 19180578
[TBL] [Abstract][Full Text] [Related]
7. Incidence of placental mosaicism leading to discrepant results between QF-PCR and karyotyping in 22,825 chorionic villus samples.
Holgado E; Liddle S; Ballard T; Levett L
Prenat Diagn; 2011 Nov; 31(11):1029-38. PubMed ID: 21755518
[TBL] [Abstract][Full Text] [Related]
8. Maternal cell contamination of prenatal samples assessed by QF-PCR genotyping.
Stojilkovic-Mikic T; Mann K; Docherty Z; Mackie Ogilvie C
Prenat Diagn; 2005 Jan; 25(1):79-83. PubMed ID: 15662689
[TBL] [Abstract][Full Text] [Related]
9. A retrospective and theoretical evaluation of rapid methods for detecting chromosome abnormalities and their implications on genetic counseling based on a series of 3868 CVS diagnoses.
Soler A; Morales C; Badenas C; Rodríguez-Revenga L; Carrió A; Margarit E; Costa D; Borrell A; Goncé A; Milà M; Sánchez A
Fetal Diagn Ther; 2008; 23(2):126-31. PubMed ID: 18046070
[TBL] [Abstract][Full Text] [Related]
10. Prenatal diagnosis of uniparental disomy 15 following trisomy 15 mosaicism.
Christian SL; Smith AC; Macha M; Black SH; Elder FF; Johnson JM; Resta RG; Surti U; Suslak L; Verp MS; Ledbetter DH
Prenat Diagn; 1996 Apr; 16(4):323-32. PubMed ID: 8734806
[TBL] [Abstract][Full Text] [Related]
11. Increased nuchal translucency, hydrops fetalis or hygroma colli. A new test strategy for early fetal aneuploidy detection.
Jenderny J; Schmidt W; Hecher K; Hackelöer BJ; Kerber S; Kochhan L; Held KR
Fetal Diagn Ther; 2001; 16(4):211-4. PubMed ID: 11399881
[TBL] [Abstract][Full Text] [Related]
12. Partial trisomy/monosomy 6q in fetal cells and CVS long-term culture not present in CVS short-term culture.
Wegner RD; Schröck E; Obladen M; Becker R; Stumm M; Sperling K
Prenat Diagn; 1996 Aug; 16(8):741-8. PubMed ID: 8878285
[TBL] [Abstract][Full Text] [Related]
13. Rapid prenatal diagnosis of aneuploidy for chromosomes 21, 18, 13, and X by quantitative fluorescence polymerase chain reaction.
Ochshorn Y; Bar-Shira A; Jonish A; Yaron Y
Fetal Diagn Ther; 2006; 21(4):326-31. PubMed ID: 16757905
[TBL] [Abstract][Full Text] [Related]
14. Prenatal detection of isochromosome 21 by QF-PCR. A comparison between FISH and traditional karyotyping.
Gole L; Lian NB; Lian NP; Rauff M; Biswas A; Choolani M
Fetal Diagn Ther; 2008; 24(1):47-50. PubMed ID: 18504381
[TBL] [Abstract][Full Text] [Related]
15. The detection of aneuploidy and maternal contamination by QF-PCR in samples undergoing prenatal diagnosis for thalassemia in Southern China.
Liao C; Yang X; Li FT; Li J; Li DZ
Eur J Obstet Gynecol Reprod Biol; 2009 Jun; 144(2):149-52. PubMed ID: 19375212
[TBL] [Abstract][Full Text] [Related]
16. Prenatal diagnosis of trisomy 20 by chorionic villus sampling (CVS): a case report with long-term outcome.
Steinberg Warren N; Soukup S; King JL; St J Dignan P
Prenat Diagn; 2001 Dec; 21(13):1111-3. PubMed ID: 11787033
[TBL] [Abstract][Full Text] [Related]
17. Rapid prenatal diagnosis of common aneuploidies in amniotic fluid using quantitative fluorescent polymerase chain reaction.
Onay H; Ugurlu T; Aykut A; Pehlivan S; Inal M; Tinar S; Ozkinay C; Ozkinay F
Gynecol Obstet Invest; 2008; 66(2):104-10. PubMed ID: 18446039
[TBL] [Abstract][Full Text] [Related]
18. Rapid prenatal diagnosis of aneuploidy using quantitative fluorescence-PCR (QF-PCR).
Ogilvie CM; Donaghue C; Fox SP; Docherty Z; Mann K
J Histochem Cytochem; 2005 Mar; 53(3):285-8. PubMed ID: 15750003
[TBL] [Abstract][Full Text] [Related]
19. The replacement of cytogenetic analysis by direct chorionic villi sampling preparation with quantitative fluorescence PCR.
Christopoulou S; Christopoulou G; Hatzaki A; Hatzipouliou A; Donoghue J; Karkaletsi M; Kaminopetros P; Sifakis S; Velissariou V
Gynecol Obstet Invest; 2009; 68(4):255-61. PubMed ID: 19776613
[TBL] [Abstract][Full Text] [Related]
20. Prenatal detection of Down's syndrome by rapid aneuploidy testing for chromosomes 13, 18, and 21 by FISH or PCR without a full karyotype: a cytogenetic risk assessment.
Caine A; Maltby AE; Parkin CA; Waters JJ; Crolla JA;
Lancet; 2005 Jul 9-15; 366(9480):123-8. PubMed ID: 16005334
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]